Novel chemistry of indole in the synthesis of heterocycles von Gribble, G. W.

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The diversity of naturally produced organohalogens von Gribble, Gordon W.

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Synthetic Oleanane and Ursane Triterpenoids with Modified Rings A and C:  A Series of Highly Active Inhibitors of Nitric Oxide Production in Mouse Macrophages von Honda, Tadashi, Rounds, BarbieAnn V, Bore, Lothar, Finlay, Heather J, Favaloro, Frank G, Suh, Nanjoo, Wang, Yongping, Sporn, Michael B, Gribble, Gordon W

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Novel triterpenoids suppress inducible nitric oxide synthase (iNOS) and inducible cyclooxygenase (COX-2) in mouse macrophages von NANJOO SUH, HONDA, T, FINLAY, H. J, BARCHOWSKY, A, WILLIAMS, C, BENOIT, N. E, XIE, Q.-W, NATHAN, C, GRIBBLE, G. W, SPORN, M. B

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A novel synthetic oleanane triterpenoid, 2-cyano-3,12-dioxoolean-1,9-dien-28-oic acid, with potent differentiating, antiproliferative, and anti-inflammatory activity von NANJOO SUH, YONGPING WANG, WILLIAMS, C. R, GENGFEI WU, DANNENBERG, A. J, FLANDERS, K. C, LETTERIO, J. J, MANGELSDORF, D. J, NATHAN, C. F, LANANH NGUYEN, PORTER, W. W, REN, R. F, HONDA, T, ROBERTS, A. B, ROCHE, N. S, SUBBARAMAIAH, K, SPORN, M. B, GRIBBLE, G. W, DMITROVSKY, E, HICKEY, W. F, MAUE, R. A, PLACE, A. E, PORTER, D. M, SPINELLA, M. J

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Design and synthesis of 2-cyano-3,12-dioxoolean-1,9-dien-28-oic acid, a novel and highly active inhibitor of nitric oxide production in mouse macrophages von Honda, Tadashi, Rounds, BarbieAnn V., Gribble, Gordon W., Suh, Nanjoo, Wang, Yongping, Sporn, Michael B.

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The Diversity of Natural Organochlorines in Living Organisms von Gribble, G. W.

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A Synthetic Triterpenoid, 2-Cyano-3,12-dioxooleana-1,9-dien-28-oic Acid (CDDO), Is a Ligand for the Peroxisome Proliferator-Activated Receptor γ von Wang, Yongping, Porter, Weston W, Suh, Nanjoo, Honda, Tadashi, Gribble, Gordon W, Leesnitzer, Lisa M, Plunket, Kelli D, Mangelsdorf, David J, Blanchard, Steven G, Willson, Timothy M, Sporn, Michael B

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Novel synthetic oleanane triterpenoids: A series of highly active inhibitors of nitric oxide production in mouse macrophages von Honda, Ta-i, Rounds, BarbieAnn V., Bore, Lothar, Favaloro, Frank G., Gribble, Gordon W., Suh, Nanjoo, Wang, Yongping, Sporn, Michael B.

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The natural production of chlorinated compounds von Gribble, Gordon W

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Amazing Organohalogens von Gribble, Gordon W

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Naturally Occurring Organohalogen Compounds--A Survey von Gribble, Gordon W

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The bortezomib/proteasome inhibitor PS-341 and triterpenoid CDDO-Im induce synergistic anti–multiple myeloma (MM) activity and overcome bortezomib resistance von Chauhan, Dharminder, Li, Guilan, Podar, Klaus, Hideshima, Teru, Shringarpure, Reshma, Catley, Laurence, Mitsiades, Constantine, Munshi, Nikhil, Tai, Yu Tzu, Suh, Nanjoo, Gribble, Gordon W., Honda, Tadashi, Schlossman, Robert, Richardson, Paul, Sporn, Michael B., Anderson, Kenneth C.

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Novel Synthetic Oleanane and Ursane Triterpenoids with Various Enone Functionalities in Ring A as Inhibitors of Nitric Oxide Production in Mouse Macrophages von Honda, Tadashi, Gribble, Gordon W, Suh, Nanjoo, Finlay, Heather J, Rounds, BarbieAnn V, Bore, Lothar, Favaloro, Frank G, Wang, Yongping, Sporn, Michael B

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Design, Synthesis, and Biological Evaluation of Biotin Conjugates of 2-Cyano-3,12-dioxooleana-1,9(11)-dien-28-oic Acid for the Isolation of the Protein Targets von Honda, Tadashi, Janosik, Tomasz, Honda, Yukiko, Han, Jie, Liby, Karen T, Williams, Charlotte R, Couch, Robin D, Anderson, Amy C, Sporn, Michael B, Gribble, Gordon W

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Bis-Suzuki reactions of 2,3-dihaloindoles. A convenient synthesis of 2,3-diarylindoles von Liu, Yanbing, Gribble, Gordon W

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Syntheses of Polybrominated Indoles from the Red Alga Laurencia brongniartii and the Brittle Star Ophiocoma erinaceus von Liu, Yanbing, Gribble, Gordon W

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Synthesis and Reactions of N-Protected 3-Nitroindoles von Pelkey, Erin T.

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The abundant natural sources and uses of chlorinated chemicals von Gribble, G W

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Synthesis of β-Boswellic Acid Analogues with a Carboxyl Group at C-17 Isolated from the Bark of Schefflera octophylla von BORE, Lothar, HONDA, Tadashi, GRIBBLE, Gordon W.

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